共查询到20条相似文献,搜索用时 15 毫秒
1.
Isao Yamaguchi Takuya Nakahara 《Journal of polymer science. Part A, Polymer chemistry》2012,50(16):3340-3349
Polythiophenes with reactive Zincke salt structure, such as PThThPy+DNP(Cl?)Th , were synthesized by the oxidation polymerization of 3′‐(4‐N‐(2,4‐dinitrophenyl)pyridinium chloride)‐2,2′:5′,2″‐terthiophene ( ThThPy+DNP(Cl?)Th ) with iron(III) chloride or copper(II) trifluoromethanesulfonate. The reaction of PThThPy+DNP(Cl?)Th with R‐NH2 (R = n‐hexyl (Hex) and phenyl (Ph)) substituted the 2,4‐dinitrophenyl group into the R group with the elimination of 2,4‐dinitroaniline to yield PThThPy+R(Cl?)Th . Similarly, model compounds, ThThPy+R(Cl?)Th (R = Hex and Ph), were also synthesized. In contrast to the photoluminescent ThThPyTh and PThThPyTh , the compounds PThThPy+DNP(Cl?)Th , PThThPy+R(Cl?)Th , and ThThPy+R(Cl?)Th showed no photoluminescence because their internal pyridinium rings acted as quenchers. Cyclic voltammetry measurements suggested that PThThPy+DNP(Cl?)Th received an electrochemical reduction of the pyridinium and 2,4‐dinitrophenyl groups and oxidation of the polymer backbone. PThThPy+DNP(Cl?)Th was electrically conductive (ρ = 2.0 × 10?6 S cm?1) in the non‐doped state. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
2.
Dmitrij Bondarev Jiří Zedník Ivana Šloufová Ahmed Sharf Marek Procházka Jiří Pfleger Jiří Vohlídal 《Journal of polymer science. Part A, Polymer chemistry》2010,48(14):3073-3081
High‐regioregular poly{3‐[6‐(1‐methylimidazolium‐3‐yl)hexyl]thiophene‐2,5‐diyl bromide}, PMHT‐Br, has been prepared by reaction of high‐regioregular (above 92%) poly[3‐(6‐bromohexyl)thiophene‐2,5‐diyl] with 1‐methylimidazole. PMHT‐Br is soluble in water and water miscible solvents such as methanol, DMSO and shows solvatochromism; λmax (nm): 423 (H2O); 435 (MeOH); 452 (DMSO). Increased absorption band broadening observed for aqueous solution as well as NMR spectra in D2O suggests a micelle‐like structure of PMHT‐Br molecules in these solutions: poly(3‐hexylthiophene) core and 1‐methylimidazolium bromide shell. Despite the disturbing effect of ionic groups, the solid‐state PMHT‐Br shows absorption maximum at 520 nm, the band edge at 660 nm (ca. 1.9 eV), and fluorescence emission with maximum at 635 nm, in a good agreement with the polymer regioregularity. Fluorescence emission maxima: λem (nm): 598 (H2O); 562 (MeOH); 574 (DMSO), occur in a vicinity of corresponding adsorption band edges. Plot of electrical conductivity of PMHT‐Br (measured under the dynamic vacuum conditions, 5 × 10?5 Pa) versus 1/T shows a break at about 70 °C same as the temperature dependence of λmax of the solid PMHT‐Br. These breaks indicate an increase in the mobility of polymer segments and ions within PMHT‐Br; however, a thermal analysis did not provide solid evidence for it. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 3073–3081, 2010 相似文献
3.
Laura Ricciotti Fabio Borbone Antonio Carella Roberto Centore Antonio Roviello Mario Barra Giuseppina Roviello Claudio Ferone Carla Minarini Pasquale Morvillo 《Journal of polymer science. Part A, Polymer chemistry》2013,51(20):4351-4360
A novel, easy, and cost‐effective synthetic procedure is reported for the production of very highly regioregular poly[3‐(4‐alkoxyphenyl)thiophene]s by means of oxidative coupling. Four copper complexes were synthesized and used as catalysts to obtain polymers with higher regioregularity compared to the previous oxidative coupling methodologies reported in the literature and similar to that obtained by McCullough and Rieke methods in the synthesis of poly‐3‐alkylthiophenes. The regioregularity of the synthesized polymers was investigated by UV–Visible characterization on polymer thin films and 1H NMR analysis. The remarkable potentialities of these polymers have emerged from field‐effect transistor mobility measurements operated on devices with bottom‐contact configuration and hexamethyldisilazane‐treated SiO2 gate dielectric, showing a well‐defined p‐type field‐effect response and maximum mobility values in air higher than 10?4 cm2 V?1 s?1. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013, 51, 4351–4360 相似文献
4.
Helmuth Peeters Thierry Verbiest Guy Koeckelberghs 《Journal of polymer science. Part A, Polymer chemistry》2009,47(7):1891-1900
The synthesis, aggregation, and optical properties of a chiral, regioregular polythiophene, substituted with a conjugated substituent, are described. The polymer was prepared using a Stille coupling reaction. The fact that the side‐chain contributes to the absorption (UV‐vis), emission (fluorescence), and redox behavior (cyclic voltammetry) of the material demonstrates that the substituent contributes to the electronic properties. It was shown that the conjugated side‐chain chirally stacks in conditions in which the polymer backbone aggregates, which demonstrates the ability of conjugated polymers to induce a (chiral) lamellar organization of conjugated moieties, present in their side‐chain. The aggregation of both the side‐chain and the backbone was monitored using UV‐vis and CD spectroscopy. Finally, it is shown that the conjugated side‐chain can selectively be oxidized, without oxidizing the polythiophene backbone. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 1891–1900, 2009 相似文献
5.
Plasma polymerization of thiophene in the presence of iodine has been performed under mild plasma conditions, in order to
obtain a thin conducting film suitable for sensing volatile chemicals. FTIR and XPS analysis have been utilized for the chemical
characterization. The low-frequency resistance response to ethanol, methanol, acetone, ethyl acetate, and ammonia vapors was
investigated showing sensitivity to polar and low molecular weight volatile chemicals. 相似文献
6.
Derya Baran Felix M. Pasker Stephan Le Blanc Gregor Schnakenburg Tayebeh Ameri Sigurd Höger Christoph J. Brabec 《Journal of polymer science. Part A, Polymer chemistry》2013,51(4):987-992
A new donor‐acceptor copolymer consisting of triazoloquinoxaline and 9,9‐dialkylfluorene units on the main chain has been synthesized, characterized and evaluated as donor material in bulk heterojunction solar cells using PC61BM as an acceptor. The resulting polymer PTQF showed good thermal stability and solubility in common organic solvents. Cyclic Voltammetry measurements showed that the PTQF has HOMO–LUMO energy levels of ?5.13 and ?3.62 eV, respectively. DFT calculations revealed that the HOMO is delocalized all over the thiophene and fluorene units and the LUMO is localized mainly on the triazole and pyrazine units. PTQF absorbs broadly in the visible region and exhibits a bandgap of 1.4 eV. Photovoltaic devices exhibited 1.7% efficiency for 1:2 PTQF:PC61BM blend ratio using Ca/Ag electrodes. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013 相似文献
7.
Cemil Alkan Leyla Aras Güngr Gündüz 《Journal of polymer science. Part A, Polymer chemistry》2006,44(19):5692-5698
A diazodiphenylene‐bridged Cu–phthalocyanine polymer was synthesized from the diazonium salt of bensidine and the Cu(II) 1,8,15,22‐tetraaminophthalocyanine complex and characterized with Fourier transform infrared, ultraviolet–visible spectroscopy, and elemental analysis. The polymer was partially soluble in organic solvents such as dimethylformamide and tetrahydrofuran. The molecular weight of the soluble part of the polymer was investigated with ebullioscopy and viscosimetry methods in tetrahydrofuran. Both methods showed that the molecular weight of the polymer was much larger than that of the complex. The conductivity of the samples was measured with a four‐prop conductivity measuring device. Iodine and hydrogen chloride were doped to the polymer, and an increase of about 104 S cm?1 in the electrical conductivity was observed. The cyclic voltammogram of the diazodiphenylene‐bridged Cu–phthalocyanine polymer in contact with a LiClO4 electrolyte exhibited two reductions and two reoxidations with high reversibility and electrochemical stability. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 5692–5698, 2006 相似文献
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Mael Nicolas Frédéric Guittard Serge Géribaldi 《Journal of polymer science. Part A, Polymer chemistry》2007,45(20):4707-4719
A series of new fluorinated polythiophenes has been synthesized by oxidative chemical and electrochemical polymerization and by Ullmann coupling. The substitution with the perfluoroalkyl alkyl chain CH2CH2C6F13 on the 3 position of the thiophene ring is performed via an ester, thioester, or amide connector, (CH2)m‐C(O)X, m = 0–2, with a view to investigating the role of the linker on the polymerization and on the properties of the corresponding polymers. The bromination of the monomers at the 2 and 5 positions allows the use of Ullmann coupling to form soluble fluorinated oligomers. The electron affinity was determined from cyclic voltammetry and a value of 3.1 eV was found for the ester derivative; such materials represent interesting candidates for use in light‐emitting devices or as an electron accepting material in photodiodes/solar cells. The oxidative polymerizations need the connector to be spaced out from the heterocycle to reduce its withdrawal effect. The ester, thioester, and amide spacer determined to a large extent the efficiency of the oxidative polymerization, and particularly the electropolymerization, as well as the solubility of the polymers formed. All the polymers were analyzed by GPC and by UV–visible and fluorescence spectroscopies. The electrochemical oxidation of the thioester and amide group prevents the formation of electroactive films by electropolymerization. But in the case of the ester group, the electroformed polymer exhibits exceptional stable superhydrophobic and lipophobic properties because of a porous surface and the presence of a fluorinated chain that confers low surface energy. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 4707–4719, 2007 相似文献
10.
Baoling Wang Fangzhong Shen Ping Lu Shi Tang Wu Zhang Shiwei Pan Meirong Liu Linlin Liu Song Qiu Yuguang Ma 《Journal of polymer science. Part A, Polymer chemistry》2008,46(9):3120-3127
This article describes the synthesis and characterization of a new ladder‐type poly (p‐phenylene) (LPFC) containing alkylcarbazole and dialkylfluorene units in backbone, and its optical and electrochemical properties as well as its light‐emitting device performance. LPFC shows the well‐defined structure, high molecular weights, excellent thermal stability, and good solubility in common organic solvents. And it also shows strongly blue emission (λmax = 465 nm) with quantum efficiency of 70% in solution, while its solid emission (λmax = 470 nm) is almost the same as its solution. Electrochemical studies show that the highest occupied molecular orbital (HOMO) energy levels of LPFC is up to 5.29 eV, which is significantly higher than that of LPPP without carbazole in backbone, indicating an enhanced ability of hole injection from anodes. Furthermore, the single layer light‐emitting device using LPFC as the active layer shows blue emission (λmax = 470 nm) with maximum luminescence of ~ 2000 cd/m2 and maximum luminance efficiency of 0.43 cd/A. The attractive properties exhibited from new ladder‐type polymer establish LPFC as a good candidate for the potential application as transporting and emitting layer in polymeric light emitting diodes. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 3120–3127, 2008 相似文献
11.
Danming Chao Rui Yang Xiaoteng Jia Hongtao Liu Shutao Wang Ce Wang Erik B. Berda 《Journal of polymer science. Part A, Polymer chemistry》2012,50(12):2330-2336
A novel multifunctional poly(aryl ether) with both pendant oligoaniline and fluorene groups (PAE‐p‐OF) was synthesized by nucleophilic polycondensation and characterized by 1H NMR, Fourier‐transform infrared spectra, and gel permeation chromatography. The polymer showed excellent solubility in common organic solvents and good thermal stability. Electrochemical and photophysical properties were also investigated using cyclic voltammetry, UV–vis, and fluorescence spectroscopies. The obtained PAE‐p‐OF exhibits satisfactory electrochromic properties with high contrast value, acceptable coloration efficiency, and moderate switching times. Moreover, the fluorescence intensity of PAE‐p‐OF was modulated by controlling oxidation degree of oligoaniline moiety, due to the energy migration occurring between oligoaniline and fluorene groups. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
12.
Won Suk Shin Sung Chul Kim Seung‐Joon Lee Han‐Su Jeon Mi‐Kyoung Kim B. Vijaya Kumar Naidu Sung‐Ho Jin Jin‐Kook Lee Jae Wook Lee Yeong‐Soon Gal 《Journal of polymer science. Part A, Polymer chemistry》2007,45(8):1394-1402
We synthesized a novel low‐band‐gap, conjugated polymer, poly[4,7‐bis(3′,3′‐diheptyl‐3,4‐propylenedioxythienyl)‐2,1,3‐benzothiadiazole] [poly(heptyl4‐PTBT)], consisting of alternating electron‐rich, diheptyl‐substituted propylene dioxythiophene and electron‐deficient 2,1,3‐benzothiadiazole units, and its photovoltaic properties were investigated. A thin film of poly(heptyl4‐PTBT) exhibited an optical band gap of 1.55 eV. A bulk‐heterojunction solar cell with indium tin oxide/poly(3,4‐ethylenedioxythiophene)/poly(heptyl4‐PTBT): methanofullerene [6,6]‐phenyl‐C61‐butyric acid methyl ester (PCBM) (1:4)/LiF/Al was fabricated with poly(heptyl4‐PTBT) as an electron donor and PCBM as an electron acceptor and showed an open‐circuit voltage, short‐circuit current density, and power conversion efficiency of 0.37 V, 3.15 mA/cm2, and 0.35% under air mass 1.5 (AM1.5G) illumination (100 mW/cm2), respectively. A solid‐state, dye‐sensitized solar cell with a SnO2:F/TiO2/N3 dye/poly(heptyl4‐PTBT)/Pt device was fabricated with poly(heptyl4‐PTBT) as a hole‐transport material. This device exhibited a high power conversion efficiency of 3.1%, which is the highest power conversion efficiency value with hole‐transport materials in dye‐sensitized solar cells to date. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 1394–1402, 2007 相似文献
13.
Yaowen Li Zaifang Li Chunyu Wang Hui Li Hongguang Lu Bin Xu Wenjing Tian 《Journal of polymer science. Part A, Polymer chemistry》2010,48(13):2765-2776
A series of novel soluble donor‐acceptor low‐bandgap‐conjugated polymers consisting of different oligothiophene (OTh) coupled to electron‐accepting moiety 2‐pyran‐4‐ylidenemalononitrile (PM)‐based unit were synthesized by Stille or Suzuki coupling polymerization. The combination of electron‐accepting PM building block with varied OThn (the number of thiophene unit increases from 3 to 5) results in enhanced π–π stacking in solid state and intramolecular charge transfer (ICT) transition, which lead to an extension of the absorption spectra of the copolymers. Cyclic voltammetry measurements and molecular orbital distribution calculations indicate that the highest occupied molecular orbitals (HOMO) energy levels could be fine‐tuned by changing the number of thiophene units of the copolymers, and the resulting copolymers possessed relatively low HOMO energy levels promising good air stability and high‐open circuit voltage (Voc) for photovoltaic application. Bulk heterojunction photovoltaic devices were fabricated by using the copolymers as donors and (6,6)‐phenyl C61‐butyric acid methyl ester as acceptor. It was found that the highest Voc reached 0.94 V, and the short circuit currents (Jsc) were improved from 1.78 to 2.54 mA/cm2, though the power conversion efficiencies of the devices were measured between 0.61 and 0.99% under simulated AM 1.5 solar irradiation of 100 mW/cm2, which indicated that this series copolymers can be promising candidates for the photovoltaic applications. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 2765–2776, 2010 相似文献
14.
Hui Chen Yong Lu Teng‐Teng Ong Xiao Hu Siu‐Choon Ng 《Journal of polymer science. Part A, Polymer chemistry》2009,47(8):2163-2171
Novel donor–acceptor type polymers consisting of alternating quaterthiophene and an electron withdrawing moiety, pyrazinyl or pyridinyl, have been prepared using Stille coupling approach with moderate yields. The polymers were highly soluble in common organic solvents such as tetrahydrofuran and chloroform. The structure and optical properties of the polymers were characterized by NMR, UV‐vis and fluorescence spectroscopy, and cyclic voltammetry, respectively. The polymer having pyrazine unit exhibited a red‐shift in both absorption and emission in comparison with those analogs containing pyridine because of strong electron withdrawing character of the pyrazinyl group. The polymer containing pyrazinyl as acceptor units also depicted decrease in its optical and electrochemical bandgap relative to those polymers containing 2,5‐ or 2,6‐pyridine moieties. The electrochemical behavior showed facile n‐doping and p‐doping properties of those polymers consisting of alternating quaterthiophene and the acceptor moiety. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 2163–2171, 2009 相似文献
15.
Synthesis and photovoltaic properties of thieno[3,4‐b]pyrazine or dithieno[3′,2′:3,4;2″,3″:5,6]benzo[1,2‐d]imidazole‐containing conjugated polymers 下载免费PDF全文
Mukhamed L. Keshtov Dmitri Yu. Godovsky Alexei R. Khokhlov Tetsunari Mizobe Hiroyuki Fujita Eisuke Goto Junya Hiyoshi Saki Nakamura Susumu Kawauchi Tomoya Higashihara Tsuyoshi Michinobu 《Journal of polymer science. Part A, Polymer chemistry》2015,53(9):1067-1075
Novel conjugated polymers composed of benzo[1,2‐b:4,5‐b′]dithiophene and thieno[3,4‐b]pyrazine or dithieno[3′,2′:3,4;2″,3″:5,6]benzo[1,2‐d]imidazole units are synthesized by Stille polycondensation. The resulting polymers display a longer wavelength absorption and well‐defined redox activities. The effective intramolecular charge‐transfer and energy levels of all polymers are elucidated by computational calculations. Bulk‐heterojunction solar cells based on these polymers as p‐type semiconductors and [6,6]‐phenyl‐C61‐butyric acid methyl ester (PC61BM) as an n‐type semiconductor are fabricated, and their photovoltaic performances are for the first time evaluated. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015 , 53, 1067–1075 相似文献
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Wen‐Hsiang Chen Kun‐Li Wang Wen‐Yi Hung Jyh‐Chiang Jiang Der‐Jang Liaw Kueir‐Rarn Lee Juin‐Yih Lai Ci‐Liang Chen 《Journal of polymer science. Part A, Polymer chemistry》2010,48(21):4654-4667
Novel bi‐triphenylamine‐containing aromatic dibromide M3 , N,N‐bis(4‐bromophenyl)‐N′,N′‐dipheny‐l,4‐phenylenediamine, was successfully synthesized. The novel conjugated polymer P1 having number‐average molecular weight of 1.31 × 104 was prepared via Suzuki coupling from the dibromide M3 and 9,9‐dioctylfluorene‐2,7‐diboronic acid bis(1,3‐propanediol) ester. Polymer P1 had excellent thermal stability associated with a high glass‐transition temperature (Tg = 141 °C). The hole‐transporting and UV‐vis‐near‐infrared electrochromic properties were examined by electrochemical and spectroelectrochemical methods. Cyclic voltammograms of the conjugated polymer films cast onto indium‐tin oxide‐coated glass substrates exhibited two reversible oxidation redox couples at E1/2 values of 0.73 and 1.13 V versus Ag/Ag+ in acetonitrile solution. The hole mobility of the conjugated polymer P1 revealed ~10?3 cm2 V?1 s?1, which is much higher than that of other conjugated polymer systems. The observed UV‐vis‐near‐infrared absorption change in the conjugated polymer film P1 at applied potentials ranging from 0.00 to 1.23 V are fully reversible and associated with strong color changes from pale yellowish in its neutral form to green and blue in its oxidized form. Using a combination of experimental study and theoretical investigation, we proposed an oxidation mechanism based on molecular orbital theory, which explains the cyclic voltammetry experimental results well. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010 相似文献
18.
Masaya Toba Takuya Nakashima Tsuyoshi Kawai 《Journal of polymer science. Part A, Polymer chemistry》2011,49(8):1895-1906
Arylenevinylene‐based π‐conjugated polymers containing imidazolium cationic units in the main chain and their model compounds were synthesized and characterized in terms of optical and electrochemical properties. 9,9‐Bisoctylfluorene, 2,5‐bisdodecyloxybenzene, and 3‐dodecylthiophene were introduced as arylene units with different donor characteristics to evaluate the effect on the highest occupied molecular orbital‐lowest unoccupied molecular orbital (HOMO‐LUMO) gap energy. The UV–vis and fluorescence spectra of cationic polymers and model compounds with iodide counter anion exhibited a significant blue shift with respect to the parent neutral molecules. X‐ray single crystal analysis for model compounds revealed that the effective π‐conjugation length of cationic model compounds decreased compared to the neutral model compounds by means of twisted conformation directed by CH‐π interactions between N‐methyl groups of imidazolium and neighboring aryl units. The cyclic voltammetry measurement suggested the negative shift of LUMO levels by the conversion of imidazole to imidazolium, indicating the electron‐accepting characteristics of cationic imidazolium unit. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
19.
Chia‐Shing Wu Chiao‐Pei Chen Yun Chen 《Journal of polymer science. Part A, Polymer chemistry》2013,51(18):3975-3984
Copoly(p‐phenylene) ( P1 ) containing pendent azacrown ether and ethylene glycol ether was prepared by the Suzuki coupling reaction and applied for chemical sensor. Poly(p‐phenylene) derivative P0 without the azacrown ether groups were also synthesized for comparative study. The photophysical and sensing properties were investigated by absorption and photoluminescence (PL) spectroscopy to elucidate the influence of the azacrown ether groups. The P1 exhibited specific selectivity and high sensitivity toward Zn2+, with the Stern‐Volmer coefficient (Ksv) being 3.66 × 106 M?1 at low concentration in mixture solvent of tetrahydrofuran and water (THF/H2O = 9/1, v/v). The P1 maintained high selectivity toward Zn2+ in the presence of fifteen interfering metal cations. This results indicate that copoly(p‐phenylene) ( P1 ) is a promising functional material for chemical sensors. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013 , 51, 3975–3984 相似文献
20.
Hava Zekiye Akpinar Yasemin Arslan Udum Levent Toppare 《Journal of polymer science. Part A, Polymer chemistry》2013,51(18):3901-3906
Two novel thiazolo[5,4‐d]thiazole containing donor–acceptor type alternating copolymers, poly[2‐(5‐(2‐decyl‐2H‐benzo[d][1,2,3]triazol‐4‐yl)thiophen‐2‐yl)‐5‐(thiophen‐2‐yl)thiazolo[5,4‐d]thiazole] (BTzTh) and poly[2‐(5‐(2‐decyl‐2H‐benzo[d][1,2,3]triazol‐4‐yl)furan‐2‐yl)‐5‐(furan‐2‐yl)thiazolo[5,4‐d]thiazole] (BTzFr) were synthesized by Stille coupling polymerization and their electrochemical and electrochromic properties were explored. Electrochemical activities of the spray‐casted polymer films were determined by cyclic voltammetry. To evaluate the effect of thiophene and furan moieties on the optical properties of the copolymers, spectroelectrochemistry studies were performed. To examine the switching abilities, copolymer films were subjected to a double potential step chronoamperometry in their local maximum absorptions. Both thiazolothiazole‐containing copolymers showed multichromic properties with low band‐gap values 1.7 and 1.9 eV for BTzTh and BTzFr, respectively. The decent electrochromical properties together with solution processability make them important candidates for electrochromic applications. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013 , 51, 3901–3906 相似文献